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Microplastic-Derived Carbon Emissions: From Granular Carbon to Dissolved Organic Carbon and Carbon Dioxide under Ultraviolet Radiation
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Researchers examined carbon emissions from microplastics during aging processes, finding that MPs release not only dissolved organic carbon but also granular carbon particles as they degrade, expanding understanding of the contribution of plastic pollution to oceanic carbon cycling and carbon budgets.
As a hydrocarbon polymer, microplastics (MPs) consisted of abundant carbon. Previous studies mostly focused on the surface degradation of MPs and the release of dissolved organic carbon (DOC) during aging processes, while the information about MP-derived carbon emission from granular carbon (GC) to DOC and carbon dioxide (CO2) is limited. This study examined the dynamic changes in MP carbon from GC loss to the formation of DOC and CO2 by selecting polystyrene (PS) and polybutylene succinate (PBS) as representative traditional and biodegradable MPs under ultraviolet (UV) radiation and mechanical abrasion. Results revealed that PS and PBS exhibited broken surfaces after UV radiation, and the mass and GC content of PS and PBS significantly decreased. The GC loss in PS and PBS was mainly converted into DOC, with only a small portion converted into CO2. The GC loss and DOC increase in PBS exceeded those in PS, while PBS exhibited lower CO2 content than PS. OH• and O2•- were identified as the key factors influencing the UV-induced degradation of PS and PBS. This study provides new insights into the carbon emissions of MPs throughout their environmental degradation lifecycle and their contribution to global carbon emissions.
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Microplastic-DerivedCarbon Emissions: From GranularCarbon to Dissolved Organic Carbon and Carbon Dioxide under UltravioletRadiation
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Researchers investigated microplastic-derived carbon emissions under ultraviolet radiation, tracking the transformation pathway from granular carbon to dissolved organic carbon and ultimately carbon dioxide, finding that UV aging drives significant carbon release from hydrocarbon polymer microplastics.
Photolysis of microplastics under ultraviolet radiation : greenhouse gas emissions.
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Researchers investigated the photodegradation of microplastics under UV radiation, measuring greenhouse gas emissions produced during polymer breakdown. The study found that microplastic photolysis releases carbon-based gases, adding a previously underappreciated contribution to atmospheric greenhouse gas budgets.
Size and Structure-Dependent Molecular Fingerprint Transformation of Microplastic-Derived Dissolved Organic Matter in Sunlit Seawater: Implication for Marine Carbon Cycles
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This study examined how the size and structure of microplastics influence the photochemical transformation of MP-derived dissolved organic matter under UV irradiation, finding that inherent plastic properties determine the molecular character of DOM released and its effects on ocean carbon cycling.
Photolysis of microplastics under ultraviolet radiation : greenhouse gas emissions.
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Researchers investigated how ultraviolet radiation drives the photolytic degradation of microplastics ranging from 1 micron to 5 mm, measuring greenhouse gas emissions produced as plastics fragment and oxidize under UV exposure. Photolysis was shown to both fragment microplastics and release gases including methane and ethylene, linking plastic degradation to climate-relevant emissions.
Solar radiation stimulates release of semi-labile dissolved organic matter from microplastics
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Researchers found that solar radiation causes microplastics to release dissolved organic matter into seawater, with low-density polyethylene releasing about five times more carbon per gram per day than polystyrene. The released organic compounds included nitrogen- and sulfur-containing molecules, and a portion overlapped with compounds found naturally in coastal waters. Incubation experiments showed that microbes could utilize 9-19% of this plastic-derived organic matter within 30 days, suggesting it becomes part of the marine carbon cycle.
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